A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17978647



Internal ID20545687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125734501..125735300hg38UCSC Ensembl
chr10:127423070..127423869hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438362
Supporting Variants
Samples
Known GenesC10orf137
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17978647
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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